GovWire

VICH consultation until 30 November 2024 on guidelines relating to the technical requirements for demonstrating genotoxic safety of residues of veterinary drugs in human food.

Reporting against VMD published standards up to 31 March 2025.

Dermipred tablets seized at East Midlands Airport.

Biheldon cat and dog wormers seized at East Midlands Airport.

Pharmaceutical Assessor vacancy, working in the regulation of veterinary medicines.

Explanation of what Pharmacovigilance means and who is responsible. These documents must be read with the Implementation Explainer at VMD Information Hub.

Explainer for the pharmaceutical industry on the implementation of Pharmacovigilance requirements during the transition time from the date the revised VMR have effect in GB to 17 May 2027.

Adored Beast products stopped at East Midlands Airport.

GIGI Vet supplements stopped at East Midlands Airport.

Guidance for the veterinary pharmaceutical industry on how to apply for and maintain a shared-label for use on veterinary medicines placed on the market in the UK and Ireland.

This is the Hub for all the Veterinary Medicines Directorate's communications on current and future regulatory changes.

Once a VMP is on the UK market an MAH must record and submit the results of their signal management process, alongside sales and worldwide authorisation status data.

Explanation of what Pharmacovigilance means and who is responsible. These documents must be read with the Implementation Explainer at VMD Information Hub.

Requirements for an Animal Test Certificate (ATC) to carry out the field trial of a veterinary medicine in animals (clinical trial) in the UK.

New legislation in force from today in Great Britain makes changes to the requirements set out in the Veterinary Medicines Regulations 2013.

Records that must be kept when supplying or administering veterinary medicines in the UK.

Guidance for prescribing vets on the use of the cascade.

Guidance on medicines for food and non-food horses and record keeping requirements including the horse passport.

You can appeal against certain decisions made by the Veterinary Medicines Directorate (VMD) that affect you.

How to report suspected illegal activity and how we will deal with these reports.

Placing a veterinary medicine on the market, including non-medicinal products, medicinal words and phrases, how to obtain advice, report non-compliance.

The legal text underpinning the regulation of manufacture, authorisation, marketing, distribution, use and post-authorisation surveillance of veterinary medicines and medicated feed.

This enforcement policy sets out the general principles and approach taken by the VMD.

How veterinary medicines can be advertised.

Explainer for businesses and persons regulated by the Veterinary Medicines Regulations 2013, as amended, on the transitional provisions included in the amending legislation: the Veterinary Medicines (Amendment etc.) Regulations 2024.

Who in the pharmaceutical industry can be a Marketing Authorisation Holder, named distributor or local representative and how to make changes to these.

Apply to register, renew, or vary a Veterinary Homeopathic Remedy.

Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.